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Structure of 89536-85-6
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(R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-methylbutanoic acid is a chiral building block featuring a stereodefined (R)-center and a protected amine. This bench-stable derivative integrates seamlessly into peptide synthesis workflows, where the tert-butoxycarbonyl group enables selective N-terminal protection. The methyl-substituted aliphatic chain enhances solubility in organic solvents, supporting efficient coupling reactions under standard conditions.
(R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-methylbutanoic acid serves as a versatile chiral building block for peptide synthesis and medicinal chemistry applications. Its tert-butyl carbamate (Boc) group enables orthogonal protection of primary amines, while the methylamino functionality provides a handle for further derivatization. The molecule exhibits excellent bench stability, facilitates straightforward purification via standard chromatographic methods, and participates reliably in amide coupling and reduction reactions within established synthetic workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: